# FDA Inspection 908043 - Genesis Biosystems, Inc - December 16, 2014

Source: https://www.keypedia.com/records/fda_inspections/genesis-biosystems-inc/e855a5cc-38ed-48c4-a42b-5a365dc9b681
Source feed: FDA_Inspections

> FDA inspection 908043 of Genesis Biosystems, Inc, December 16, 2014. Classification: Official Action Indicated (OAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 908043
- Company Name: Genesis Biosystems, Inc
- Inspection Date: 2014-12-16
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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- [FDA Inspection 1028385 - 2017-08-31](https://www.keypedia.com/records/fda_inspections/genesis-biosystems-inc/9dab9818-70aa-4346-aaa4-1b2465373a3e)
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- FDA Inspection 838279 - 2013-06-27

Company: https://www.keypedia.com/companies/genesis-biosystems-inc/3e6cf839-9bf8-4efa-ab65-d78786001597

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
